"Laboratory of Medical Genetics, National & Kapodistrian University of - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1299586	NM_000384.3(APOB):c.11397del (p.Lys3799fs)	APOB (K3799fs)	Deletion (frameshift variant)	Hypercholesterolemia, autosomal dominant, type B	GPathogenic
Select item 1299572	NM_000384.3(APOB):c.1003del (p.Lys334_Leu335insTer)	APOB	Deletion (nonsense)	Familial hypobetalipoproteinemia 1	GPathogenic